Patient support apparatus having alert light

ABSTRACT

A patient support apparatus includes a bed frame having a head end and a foot end and control circuitry carried by the bed frame. The control circuitry receives information about conditions of the patient support apparatus. A light is coupled to the bed frame adjacent the foot end and is coupled to the control circuitry. The light is in a first state when the patient support apparatus is operating normally and the light is in a second state when the control circuitry detects an alert condition.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No.13/334,161, filed Dec. 22, 2011, issued as U.S. Pat. No. 8,464,380,which is a continuation of U.S. application Ser. No. 11/994,478, filedOct. 8, 2008, issued as U.S. Pat. No. 8,117,701, which is the U.S.national phase of PCT/US2006/026788, filed Jul. 7, 2006. PCTUS2006/026788 claims priority to U.S. Provisional Patent Application No.60/697,708, filed Jul. 8, 2005. The entire disclosures of bothPCT/US2006/026788 and U.S. Provisional Patent Application No. 60/697,708are hereby incorporated by reference herein. The present application isrelated to U.S. patent application Ser. No. 11/119,980, entitledPRESSURE RELIEF SURFACE, and U.S. patent application Ser. No.11/119,991, entitled PATIENT SUPPORT HAVING REAL TIME PRESSURE CONTROL,and U.S. patent application Ser. No. 11/119,635, entitled LACK OFPATIENT MOVEMENT MONITOR AND METHOD, and U.S. patent application Ser.No. 11/120,080, entitled PATIENT SUPPORT, all of which were filed on May2, 2005, all of which are assigned to the assignee of the presentinvention, and all of which are incorporated herein by this reference.

The present application is also related to U.S. Provisional PatentApplication No. 60/636,252, entitled QUICK CONNECTOR FOR MULTIMEDIA,filed Dec. 15, 2004, which is assigned to the assignee of the presentinvention and incorporated herein by this reference.

The present application is also related to U.S. Provisional PatentApplication No. 60/697,748, entitled PRESSURE CONTROL FOR A HOSPITALBED, filed Jul. 8, 2005 and corresponding PCT Patent Application No.PCT/US2006/026787, filed Jul. 7, 2006, and U.S. Provisional PatentApplication No. 60/697,723, entitled PRESSURE RELIEF SUPPORT SURFACE,filed Jul. 8, 2005 and corresponding PCT Patent Application No.PCT/US2006/026620, filed the Jul. 7, 2006, all of which are incorporatedherein by this reference.

The present application is also related to U.S. Provisional PatentApplication No. 60/734,942, entitled PNEUMATIC VALVE ASSEMBLY FOR APATIENT SUPPORT, filed Nov. 9, 2005, assigned to the assignee of thepresent invention and incorporated herein by this reference.

BACKGROUND

The present disclosure relates to a control unit for a device forsupporting a patient, such as a mattress. In particular, the presentdisclosure relates to a control unit for a patient support appropriatefor use in hospitals, acute care facilities, and other patient careenvironments.

SUMMARY

A control unit for a patient support is provided. The control unitincludes a housing adaptable to be removably coupled to a patientsupport, the housing defining an interior region including a controller,and an air supply including a first portion operably coupled to thecontroller to provide high volume, low pressure air to a first interiorportion of the patient support, and a second portion operably coupled tothe controller to provide low volume, high pressure air to a secondinterior portion of the patient support.

The first air supply portion may include a blower and the second airsupply portion may include a compressor. A hose connector coupled to theair supply may also be included. The hose connector may include a firstconnector portion coupled to the first air supply portion and a secondconnector portion coupled to the second air supply portion.

A display portion pivotably coupled to the housing may also be included.

A plurality of communications ports including a wireless connectivityport may also be included.

A memory port configured to receive a removable memory card may also beincluded.

An identification tag coupled to the housing may also be included.

In another embodiment, a control unit for a patient support is provided.The control unit includes a housing adaptable to be removably coupled toa patient support, the housing defining an interior region including acontroller and an air supply, and a display portion pivotably coupled tothe housing, the display portion being movable with respect to thehousing between a raised position and a lowered position, the displayportion including a video display and a touchscreen user interface.

The display portion may include a wireless access port. The displayportion may include a memory port configured to receive removablememory.

A friction hinge coupled between the display portion and the housing mayalso be included.

The angle of the display portion with respect to the housing when thedisplay portion is in the raised position may be at least 180 degrees.

A detent configured to hold the display portion in the lowered positionmay also be included.

The user interface may include a graphical depiction of a patientsupport which varies based on the presence or absence of a patient onthe patient support.

In yet another embodiment, a control unit for a patient support isprovided. The control unit includes a housing adaptable to be coupled toa patient support, the housing defining an interior region, a controllerlocated in the interior region, a user interface coupled to the housing,and a light bar coupled to the housing, the light bar being controllableby the controller to selectively illuminate in one of a plurality ofmodes.

Each of the plurality of modes may be indicative of a differentoperating condition of the control unit. The light bar may illuminate ina first mode if the patient support is in CPR position. The light barmay illuminate in a second mode if the control unit is in need ofservice. The light bar may illuminate in a third mode if the controlunit is powered on and operating normally. The light bar may illuminatein a fourth mode if an alarm is activated. The light bar may beilluminated in a different color and/or intermittently (i.e. flashing)to indicate a particular operational mode, or for other reasons.

In still another embodiment, a control unit for a patient support isprovided. The control unit includes a base portion including acontroller and an air supply, and a display portion configured todisplay a graphical user interface including at least one graphicaldepiction that automatically changes in response to a change in anoperating condition of the patient support.

The graphical depiction may be of a patient support and the graphicaldepiction may change automatically in response to a person beingpositioned on the patient support. The graphical depiction may be of apatient support and the graphical depiction may change automatically inresponse to articulation of a portion of the patient support. Thegraphical depiction may be of a patient support and the graphicaldepiction may change automatically in response to a change in inflationof the patient support. The graphical depiction may be of a pressure mapfor a patient support and the pressure map may change automatically inresponse to patient movement.

BRIEF DESCRIPTION OF THE DRAWINGS

Aspects of the present invention are more particularly described belowwith reference to the following figures, which illustrate exemplaryembodiments of the present invention:

FIG. 1 is a perspective view of a control unit in accordance with thepresent invention, shown supported by a footboard portion of anexemplary hospital bed.

FIG. 2 is a perspective view of a control unit for a patient supportpositioned on a footboard portion of an exemplary hospital bed, with aportion of the patient support being cut away to show interiorcomponents of the patient support;

FIG. 3 is a perspective view of the exemplary patient support, with aportion being cut away to show interior components of the patientsupport;

FIG. 4 is an exploded view of components of the exemplary patientsupport;

FIG. 5 is a schematic view of air zones of the exemplary patient supportand couplings to a control unit;

FIGS. 6 and 7 are schematic diagrams of portions of a control system forthe exemplary patient support;

FIG. 8 is an exploded view of an exemplary pneumatic assembly;

FIG. 9 is a perspective view of the pneumatic assembly of FIG. 8;

FIG. 10 illustrates a functional block diagram illustrating the headzone and seat zone sensors and other system components coupled to acommunication network;

FIG. 11 illustrates a block diagram for a control system in accordancewith the present invention including an algorithm control unit;

FIG. 12 is a perspective view of a control unit in accordance with thepresent invention;

FIG. 13 is a perspective view of a control unit with a display portionrotated upward;

FIG. 14 is an exploded perspective view of a control unit housing andcoupling of a display portion to the control unit housing;

FIG. 15 is a perspective view of a control unit with a portion of thehousing removed to show internal components;

FIG. 16 is a perspective view of a control unit with a portion of thehousing removed to show other internal components;

FIG. 17 is an exploded perspective view of internal components of acontrol unit from the perspective of a person facing the front side ofthe control unit;

FIG. 18 is an exploded perspective view of internal components of acontrol unit from the perspective of a person facing the back side ofthe control unit;

FIG. 19 is a schematic block diagram of an internal architecture of acontrol unit;

FIG. 20 is a schematic block diagram of an internal architecture of adisplay board of a control unit;

FIG. 21 is a schematic block diagram of an internal architecture of analgorithm control board of a control unit;

FIGS. 22 A-D are exemplary user interfaces for a main display screen ofa control unit;

FIG. 23 is an exemplary user interface for a pull down menu for acontrol unit;

FIG. 24 is an exemplary user interface for configuring alarm settings ofa control unit;

FIGS. 25 A-D are exemplary user interfaces for configuring selectedalarm types;

FIGS. 26 A-D are exemplary user interfaces for configuring other alarmtypes;

FIG. 27 is an exemplary user interface for a surface pressure map;

FIGS. 28 A-D are exemplary user interfaces for configuring a firmnessoverride feature;

FIGS. 29 A-B are exemplary user interfaces for viewing instructionalmaterial relating to a patient support;

FIGS. 30 A-F are exemplary user interfaces for monitoring a pressurerelief feature;

FIGS. 31A-D are exemplary user interfaces for monitoring a turn-assistfeature;

FIGS. 32A-B are exemplary user interfaces for monitoring a CPR feature;

FIG. 33 is an exemplary user interface for initial mattress setup; and

FIG. 34 is an exemplary user interface for entering patient weight.

Corresponding reference characters indicate corresponding partsthroughout the several views. Although the exemplification set outherein illustrates an embodiment of the invention, in one form, theembodiment disclosed below is not intended to be exhaustive or to beconstrued as limiting the scope of the invention to the precise formdisclosed.

DETAILED DESCRIPTION

FIG. 1 shows an embodiment of a control unit 42 positioned on anexemplary bed 2. Control unit 42 is configured to control certainautomated features of mattress 10. Mattress 10 may be any suitablemattress having one or more automated features.

FIG. 2 shows an illustrative embodiment of a patient support or mattress10 having automated features in accordance with the present invention.Patient support 10 can accommodate a patient of any size, weight, heightor width. It is also within the scope of the present invention toaccommodate bariatric patients of up to 1000 pounds or more. Toaccommodate patients of varied sizes, the patient support may include awidth of up to 50 inches or more.

Patient support 10 is positioned on or supported by an exemplary bed 2.Bed 2, as illustrated, is a hospital bed including a frame 4, aheadboard 36, a footboard 38, and a plurality of siderails 40.

Frame 4 of the exemplary bed 2 generally includes a deck 6 supported bya base 8. Deck 6 includes one or more deck sections (not shown), some orall of which may be articulating sections, i.e., pivotable with respectto base 8. In general, patient support 10 is configured to be supportedby deck 6.

Patient support 10 has an associated control unit 42, which controlsautomated features of patient support 10, such as inflation anddeflation of internal components of patient support 10. Control unit 42includes a user interface 44, which enables caregivers, servicetechnicians, and/or service providers to configure patient support 10according to the needs of a particular patient. For example, supportcharacteristics of patient support 10 may be adjusted according to thesize, weight, position, or activity level of the patient. User interface44 is password-protected or otherwise designed to prevent access byunauthorized persons.

User interface 44 also enables patient support 10 to be adapted todifferent bed configurations. For example, deck 6 may be a flat deck ora step or recessed deck. An end user may select the appropriate deckconfiguration via user interface 44. Inflation or deflation of specificmattress components may occur in response to user selection of ahospital bed frame or deck configuration.

Referring now to FIG. 3, patient support 10 has a head end 32 generallyconfigured to support a patient's head and/or upper body region, and afoot end 34 generally configured to support a patient's feet and/orlower body region. Patient support 10 includes a cover 12 which definesan interior region 14. In the illustrated embodiment, interior region 14includes a first layer 20, a second layer 50, and a third layer 52.Other embodiments of the present invention may not include all three ofthese layers, or may include additional layers.

In the illustrated embodiment, first layer 20 includes a supportmaterial, second layer 50 includes a plurality of vertically-orientedinflatable bladders located underneath the first layer 20, and thirdlayer 52 includes a plurality of pressure sensors located underneath thevertical bladders of second layer 50.

Also located within interior region 14 of the exemplary patient supportare a plurality of bolsters 54, one or more filler portions 56, and apneumatic valve control box 58. A fire-resistant material (not shown)may also be included in the interior region 14.

Patient support 10 may be coupled to deck 6 by one or more couplers 46.Illustratively, couplers 46 are conventional woven or knit or fabricstraps including a D-ring or hook and loop assembly or Velcro™-brandstrip or similar fastener. Other suitable couplers, such as buttons,snaps, or tethers may also be used.

Components of the illustrated embodiment of a patient support inaccordance with the present invention are shown in exploded view in FIG.4. This embodiment of patient support 10 includes a top cover portion 16and a bottom cover portion 18. Top cover portion 16 and bottom coverportion 18 couple together by conventional means (such as zipper,Velcro™ strips, snaps, buttons, or other suitable fastener) to formcover 12, which defines interior region 14. While a plurality of layers,features, and/or components are illustrated within interior region 14,neither the illustrated embodiment of patient support 10 nor the presentinvention requires all of the illustrated components to be present.

A first support layer 20 is located below top cover portion 16 ininterior region 14. First support layer 20 includes one or morematerials, structures, or fabrics suitable for supporting a patient,such as foam, inflatable bladders, or three-dimensional material.Suitable three-dimensional materials include Spacenet, Tytex, and/orsimilar materials.

Returning to FIG. 4, a second support layer 50 including one or moreinflatable bladder assemblies, is located underneath the first supportlayer 20. The illustrated embodiment of the second support layer 50includes first, second and third bladder assemblies, namely, a headsection bladder assembly 60, a seat section bladder assembly 62, and afoot section bladder assembly 64. Other embodiments include only onebladder assembly extending from head end 32 to foot end 34, and otherarrangements of multiple bladder assemblies, for example, including anadditional thigh section bladder assembly. In general, bladderassemblies disclosed herein are formed from a lightweight, flexibleair-impermeable material such as a polymeric material like polyurethane,urethane-coated fabric, vinyl, or rubber.

A pressure-sensing layer 69 illustratively including first and secondsensor pads, namely a head sensor pad 68 and a seat sensor pad 70, ispositioned underneath bladder assemblies 60, 62, 64. Head sensor pad 68is generally aligned underneath head section bladder assembly 60, andseat sensor pad 70 is generally aligned underneath seat section bladderassembly 62, as shown. Head filler 66 may be positioned adjacent headsensor pad 68 near head end 32 so as to properly position head sensorpad 68 underneath the region of patient support 10 most likely tosupport the head or upper body section of the patient. In otherembodiments, a single sensor pad or additional sensor pads, for example,located underneath foot section bladder assembly 64, and/or differentalignments of the sensor pads, are provided.

In the illustrated embodiment, a turn-assist cushion or turning bladderor rotational bladder 74 is located below sensor pads 68, 70. Theexemplary turn-assist cushion 74 shown in FIG. 4 includes a pair ofinflatable bladders 74 a, 74 b. Another suitable rotational bladder 74is a bellows-shaped bladder. Another suitable turn-assist cushion isdisclosed in, for example, U.S. Pat. No. 6,499,167 to Ellis, et al.,which patent is owned by the assignee of the present invention andincorporated herein by this reference.

A plurality of other support components 66, 72, 76, 78, 80, 84, 86, 90are also provided in the mattress of FIG. 4. One or more of thesesupport components are provided to enable patient support 10 to be usedin connection with a variety of different bed frames, in particular, avariety of bed frames having different deck configurations. One or moreof these support components may be selectively inflated or deflated oradded to or removed from patient support 10 in order to conform patientsupport 10 to a particular deck configuration, such as a step orrecessed deck or a flat deck.

The support components illustrated in FIG. 4 are made of foam,inflatable bladders, three-dimensional material, other suitable supportmaterial, or a combination of these. For example, as illustrated, headfiller 66 includes a plurality of foam ribs extending transverselyacross patient support 10. Head filler 66 could also be an inflatablebladder. Filler portion 72 includes a foam layer positionedsubstantially underneath the sensor pads 68, 70 and extendingtransversely across the patient support 10. In the illustratedembodiment, filler portion 72 includes a very firm foam, such aspolyethylene closed-cell foam, with a ½-inch thickness.

Head bolster assembly 76, seat bolster assembly 78, and foot sectionbolster assembly 86 each include longitudinally-oriented inflatablebladders spaced apart by coupler plates 144.

As illustrated, first foot filler portion 80 includes a plurality ofinflatable bladders extending transversely across patient support 10,and second foot filler portion 84 includes a foam member, illustrativelywith portions cut out to allow for retractability of the foot section orfor other reasons. Deck filler portion 90 includes a plurality oftransversely-extending inflatable bladders. As illustrated, deck fillerportion 90 includes two bladder sections located beneath the head andseat sections of the mattress, respectively, and is located outside ofcover 12. Deck filler portion 90 may include one or more bladderregions, or may be located within interior region 14, without departingfrom the scope of the present invention.

Also provided in the illustrated embodiment are a pneumatic valve box 58and an air supply tube assembly 82. Receptacle 88 is sized to housepneumatic valve box 58. In the illustrated embodiment, receptacle 88 iscoupled to bottom cover portion 18 by Velcro™ strips. Pneumatic box 58and tube assembly 82 are described below with reference to FIG. 5, andFIGS. 8-9.

In the illustrated embodiment, support layer 20 includes a breathable orair permeable material which provides cushioning or support for apatient positioned thereon and allows for circulation of air underneatha patient. The circulated air may be at ambient temperature, or may becooled or warmed in order to achieve desired therapeutic effects.

Also in the illustrated embodiment, support layer 20 includes or isenclosed in a low friction air permeable material (such as spandex,nylon, or similar material) enclosure that allows support layer 20 tomove with movement of a patient on patient support 10, in order toreduce shear forces, for instance. In other embodiments, the enclosureis made of a non-air permeable, moisture/vapor permeable material suchas Teflon or urethane-coated fabric.

A schematic diagram of the pneumatic control system of patient support10 is shown in FIG. 5. Reading FIG. 5 from left to right, there is showna simplified top view of patient support 10 with portions removed tobetter illustrate the various air zones 160, a simplified side view ofpatient support 10, a schematic representation of pneumatic valve box58, a schematic representation of control unit 42, and air lines 146,148, 150 linking control unit 42, valve box 58, and air zones 160.

As shown in FIG. 5, air zones 160 of patient support 10 are assigned asfollows: zone 1 corresponds to head section bladder assembly 60, zone 2corresponds to seat section bladder assembly 62, zone 3 corresponds tofoot section bladder assembly 64, zone 4 corresponds to upper sidebolsters 140, zone 5 corresponds to lower side bolsters 142, zone 6corresponds to upper foot bolsters 140, zone 7 corresponds to lower footbolsters 142, zone 8 corresponds to first turn-assist bladder 74, zone 9corresponds to second turn-assist bladder 74, zone 10 corresponds todeck filler 90, and zone 11 corresponds to foot filler 80.

An air line 150 couples each zone 160 to a valve assembly 162 in valvebox 58. Valve box 58 is located in the foot section 34 of patientsupport 10. Illustratively, valve box 58 is releasably coupled to bottomportion 18 of cover 12 in interior region 14, i.e., by one or moreVelcro™-brand fasteners or other suitable coupler.

Each air line 150 is coupled at one end to an inlet port 135 on thecorresponding bladder or bladder assembly. Each air line 150 is coupledat its other end to a valve assembly 162. Each valve assembly 162includes first or fill valve 163 and a second or vent valve 165. Firstvalves 163 are coupled to air supply 152 of control unit 42 by air lines148. First valves 163 thereby operate to control inflation of thecorresponding zone 160 i.e. to fill the zone with air. Second valves 165operate to at least partially deflate or vent the corresponding zone160, for example, if the internal air pressure of the zone 160 exceeds apredetermined maximum, or if deflation is necessary or desirable inother circumstances (such as a medical emergency, or for transport ofpatient support 10).

Each valve 163, 165 has an open mode 224 and a closed mode 226, and aswitching mechanism 228 (such as a spring) that switches the value fromone mode to another based on control signals from control unit 42. Inclosed mode 226, air flows from air supply 152 through the value 163 tothe respective zone 160 to inflate the corresponding bladders, or in thecase of vent valves 165, from the zone 160 to atmosphere. In open mode224, no inflation or deflation occurs.

In the illustrated embodiment, an emergency vent valve 230 is providedto enable quick deflation of turning bladders 74 which draws air fromatmosphere through a filter 164 and also vents air to atmosphere throughfilter 164. Air supply 152 is an air pump, compressor, blower, or othersuitable air source.

Air supply 152 is coupled to a switch valve 166 by air line 146. Switchvalve 166 operates to control whether inflation or deflation of a zoneoccurs. An optional proportional valve 171 may be coupled to air line148 to facilitate smooth inflation or deflation of turn-assist bladders74, or for other reasons.

In the illustrated embodiment, valve box 58 includes a first valvemodule 156 and a second valve module 158. First valve module 156includes valves generally associated with a patient's first side andsecond valve module 158 includes valves generally associated with apatient's second side.

The various zones 160 are separately inflatable. Certain of the zones160 are inflated or deflated to allow patient support 10 to conform todifferent bed frame configurations. For example, the deck filler 90(zone 10 in FIG. 5) is inflated to conform patient support 10 to certainbed frame configurations, such as step deck configurations including theTotalCare™ and CareAssist™ bed frames, made by Hill-Rom, Inc., theassignee of the present invention, but is deflated when patient support10 is used with a flat deck bed frame, such as the Advanta™ bed made byHill-Rom, Inc. As another example, the foot filler 80 (zone 11 in FIG.5) is inflated when patient support 10 is used with the VersaCare™,TotalCare™, or CareAssist™ beds, but the lower side bolsters 142 (zone 5in FIG. 5) are not inflated when patient support 10 is used with aVersaCare™ bed. As still another example, the lower foot bolsters 142(zone 7 in FIG. 5) are inflated when patient support 10 is used on flatdecks or other bed frames, including the Advanta™ and VersaCare™ bedframes made by Hill-Rom, Inc.

FIGS. 6 and 7 are a simplified schematic diagram of a control system fora patient support or mattress 10 in accordance with the presentinvention. FIG. 6 schematically illustrates the patient support 10including the various components of patient support 10 whereas FIG. 7schematically illustrates the control unit 42 and various componentstherein. The patient support 10 includes the sensor pad 52 which iscoupled to the pneumatic valve control box 58 as previously described.The sensor pad 52 includes a head sensor pad 68 and a seat sensor pad70. The head sensor pad 68 is located at the head end 32 of the mattress10. The seat sensor pad 70 is located at a middle portion of themattress 10 which is located between the head end 32 and a location ofthe pneumatic valve control box 58. The seat sensor pad 70 is locatedsuch that a patient laying upon the mattress 10 may have its middleportion or seat portion located thereon when in a reclined state. Inaddition, when the head end 32 of the mattress 10 is elevated, the seatportion of the patient is located above the seat sensor pad 70. The headsensor pad 68 is located beneath the head section bladder assembly 60and the seat sensor pad 70 is located beneath the seat section bladderassembly 62. Each one of the sensors of the head sensor pad 68 or theseat sensor pad 70 is located beneath or at least adjacent to one of theupstanding cylindrical bladders or cushions 50. A head angle sensor 502is coupled to the control box 58 where signals received from the sensormay provide head angle information and pressure adjustment informationfor adjusting pressure in the seat bladders 62.

The sensor pad 52 is coupled through the associated cabling to thepneumatic control box 58. The pneumatic control box 58 includes amultiplexer 508 coupled to the head sensor pad 68 and the seat sensorpad 70 through a signal and control line 510. The multiplexer board 508is also coupled to an air control board 512 which is in turn coupled toa first valve block 514 and a second valve block 516. Acommunication/power line 518 is coupled to the control unit 42 of FIG.7. Likewise, a ventilation supply line 520 which provides for air flowthrough the patient support 10 for cooling as well as removing moisturefrom the patient is also coupled to the control unit 42 of FIG. 7. Anair pressure/vacuum supply line 522 for inflating or deflating airbladders is coupled to the control unit 42 as well.

The control unit 42 of FIG. 7 includes the display 44, which displaysuser interface screens, and a user interface input device 524 forinputting to the control unit 42 user selectable information, such asthe selection of various functions or features of the present device.The selections made on the user interface input device 524 controlvarious aspects of the operation of the patient support 10, which caninclude selectable pressure control of various bladders within themattress 10, control of the deck 6, for instance to put the bed 2 in ahead elevated position, as well as displaying the current state of themattress or deck position, and other features.

An algorithm control board 526 is coupled to the user interface inputdevice 524. The algorithm control board 526 receives user generatedinput signals received through the input device 524 upon the selectionof such functions by the user. The input device 524 can include avariety of input devices, such as pressure activated push buttons, atouchscreen, as well as voice activated or other device selectableinputs. The algorithm control board 526 upon receipt of the variouscontrol signals through the user input device 524 controls not only theoperation of the mattress 10 but also a variety of other devices whichare incorporated into the control unit 42. For instance, the algorithmcontrol board 526 is coupled to a display board 528 which sends signalsto the display 44 to which it is coupled. The display board 528 is alsoconnected to an output device, e.g., a speaker 530, which generatesaudible signals which might indicate the selection of various featuresat the input device 24 or indicate a status of a patient positioned onpatient support (e.g. exiting) or indicate a status of therapy beingprovided to the patient (e.g., rotational therapy complete). Thealgorithm control board 526 receives the required power from powersupply 532 which includes an AC input module 534, typically coupled to awall outlet within a hospital room or other patient care or healthcarefacility.

The algorithm control board 526 is coupled to an air supply, which, inthe illustrated embodiment includes a compressor 536 and a blower 538.Both the compressor 536 and the blower 538 receive control signalsgenerated by the algorithm control board 526. The compressor 536 is usedto inflate the air bladders in accordance with instructions receivedfrom the algorithm control board 526. The blower 538 is used for aircirculation which is provided through the ventilation supply line 520 tothe mattress 10. It is, however, possible that the compressor 536 may beused to both inflate the bladders and to circulate the air within themattress 10. A pressure/vacuum switch valve 540 is coupled to thecompressor 536 which is switched to provide for the application of airpressure or a vacuum to the mattress 10. A muffler 541 is coupled to thevalve 540. In the pressure position, air pressure is applied to all or aportion of the mattress 10 to inflate the mattress or portion thereoffor support of the patient. In the vacuum position, the valve 540 isused to apply a vacuum to the bladders therein such that the mattressmay be placed in a collapsed state for moving to another location or forproviding a CPR function, for example. A CPR button 542 is coupled tothe algorithm control board 526.

An identification tag 544 may also be associated with the control unit42. The identification tag 544 may be affixed to an exterior surface ofthe control unit housing, or may be installed within the interior regionof the control unit housing. The ID tag may include bar code, ormagnetic strip, or may generate an infrared, radio frequency, or othersuitable electromagnetic signal indicating a unique identifierassociated with the control unit 42. Such unique identifier may be usedto locate, track, or monitor the status of the control unit, forexample, using a locating and tracking system. One example of such alocating and tracking system is disclosed in U.S. Pat. No. 6,462,656 toUlrich, et al., assigned to the assignee of the present invention andincorporated herein by this reference.

As illustrated, the algorithm control board 526, the compressor 536, theblower 538, and the user input device or user control module 524 arelocated externally to the mattress and are a part of the control unit42, which may be located or removably positioned on the footboard 38 asshown in FIG. 1. The sensors and sensor pad 52, the pneumatic valvecontrol box 58, and the air control board or microprocessor 512 forcontrolling the valves and the sensor pad system 52 are located withinthe mattress 10. It is within the present scope of the invention tolocate some of these devices within different sections of the overallsystem, for instance, such that the algorithm control board 526 could belocated within the mattress 10 or the air control board 512 could belocated within the control unit 42. Also, control box 58 could becombined with control unit 42 and be positioned outside the mattress 10.

As shown in FIGS. 8-9, one embodiment of control box 58 includes amultiplexer 252 and an air control board 250. Control board 250 iscoupled to multiplexer 252 by a jumper 254. Multiplexer 252 is furthercoupled to head sensor pad 68 and seat sensor pad 70 through a signaland control line (not shown). Control board 250 is also coupled to firstvalve module 156 and second valve module 158 by wire leads 251. Acommunication/power line 258 couples control board 250 to the controlunit 42. Communication line 258 couples to a communication plug 259 ofcontrol board 250. Jumper 254 couples multiplexer 252 to control board250 for power and access to communication line 258. Wire leads 251provide actuation power to first and second valve modules 156, 158.

An angle sensor cable 256 is provided to send a signal from a head anglesensor 502 to the control board 250. Angle sensor cable 256 couples toan angle plug 257 of control board 250. In the illustrated embodiment,head angle sensor 502 is located within head bolster assembly 76. Headangle sensor 502 indicates the angle of elevation of the head end 32 ofbed 2 as the head section of the frame 4 articulates upwardly raisingthe patient's head or downwardly lowering the patient's head. In oneembodiment, angle sensor 502 transmits the angle of head end 32 to allnodes or circuit boards within the mattress control system 42, 58. Anglesensor 502 generates an indication or indicator signal when head end 32is at an angle of at least 5.degree., at least 30.degree., and at least45.degree. The head angle indication is transmitted to the control unit42 which evaluates and processes the signal. When head end 32 is at anangle above 30.degree. turn assist 74 becomes inoperative primarily forpatient safety reasons. When head end 32 is at an angle above 45.degree.information is transmitted to control unit 42 for use in the algorithms.The 5.degree. angle indication is primarily to ensure relative flatnessof patient support 10. In the illustrated embodiment, angle sensor 502is a ball switch or string potentiometer.

As discussed above, first and second valve modules 156, 158 include fillvalves 163 and vent valves 165. First valve module 156 includes fillvalves 163 a-f and vent valves 165 a-f. Second valve module 156 includesfill valves 163 g-l and vent valves 165 g-l. Fill valves 163 a-l andvent valves 165 a-l are 12 Volt 7 Watt solenoid direct active poppetstyle valves in the illustrated embodiment. Control board 252 is able toactuate each fill valve 163 a-l and vent valve 165 a-l independently orsimultaneously. Fill valves 163 a-l and vent valves 165 a-l are all ableto be operated at the same time. In operation to initiate each valve163, 165, control board 250 sends a signal to the valve to be operated.The signal causes a coil (not shown) within each valve to energize for ½second and then switches to pulsate power (i.e., turn on and off at ahigh rate) to save power during activation. The activation in turn causethe valve to either open or close depending on which valve is initiated.

Fill valves 163 are coupled to air supply 152 of control unit 42 bysecond air line 148. Air line 148 includes an outer box line assembly260 and an inner box line assembly 262. Outer box line assembly 260includes an exterior inlet hose 264 and an elbow 266 coupled to exteriorinlet hose 264. Inner box line assembly 262 includes an interior inlethose 268 coupled to elbow 266, a union tee connector 270, a first modulehose 272, and a second module hose 274. Connector 270 includes a firstopening 276 to receive interior inlet hose 268, a second opening 278 toreceive first module hose 272, and a third opening 280 to receive secondmodule hose 274. First and second module hoses 272, 274 each couplethrough a male coupler 282 to first and second valve modules 156, 158respectively. In operation, air from air supply 152 travels throughsupply line 148, enters outer box line assembly 260 through exteriorinlet hose 264 and passes through elbow 266 to interior inlet hose 268.The air then travels from inlet hose 268 to union tee connector 270where the air is divided into first module hose 272 and second modulehose 274. The air passes through first and second module hoses 272, 274into first and second valve modules 156, 158 respectively. The operationof first and second valve modules 156, 158 is described below.

Control box 58 includes a base 284, a cover 286, and a tray 288. Cover286 includes a plurality of fasteners (i.e., screws) 290. Base 284includes a plurality of threaded cover posts 292. Cover posts 292 areconfigured to receive screws 290 to couple cover 286 to base 284. Cover286 and base 284 define an inner region 298. Tray 288 couples to base284 with a plurality of rivets 291 riveted through a plurality of rivetholes 293 located on tray 288 and base 284.

Inner box line assembly 262, first valve module 156, second valve module158, control board 250, and multiplexer 252 are contained within innerregion 298. Base 284 further includes a plurality of control board posts294, a plurality of multiplexer posts 296, and a plurality of moduleposts 300. First and second valve modules 156, 158 are coupled to moduleposts 300 by shoulder screws 302 and washers 304. Control board 250 andmultiplexer 252 are respectively coupled to control board posts 294 andmultiplexer posts 296 by a plurality of snap mounts 306.

First and second valve modules 156, 158 attach to third air lines 150 a,b, d-f, and g-l through a plurality of couplers 308. Couplers 308include a first end 310 and a second end 312. Third air lines 150 a, b,d-f, and g-l each include a fitting (not shown) receivable by second end312. Each first end 310 mounts to a port 314 in first and second valvemodules 156, 158. First end 310 mounts through a plurality of openings316 in base 284.

A plurality of feedback couplers 318 mount through a plurality offeedback openings 320 in base 284. Feedback couplers 318 include a firstfeedback end 322 and a second feedback end 324. First feedback end 322couples to a feedback line (not shown) that in turn couples to afeedback port 135 located on each air zone 160. Second feedback end 324receives a feedback transfer line 326. Each transfer line 326 couples toa pressure transducer 328 located on the control board 250. Pressuretransducer 328 receives the pressure from each air zone 160 andtransmits to control unit 42 a pressure data signal representing theinternal air pressure of the zone 160. Control unit 42 uses thesepressure signals to determine the appropriate pressures for certainmattress functions such as CPR, patient transfer, and max-inflate.Pressure signals from the transducer 328 coupled to the foot zone 160 kare also used to maintain optimal pressure in foot zone 160 k. In theillustrated embodiment, pressure in foot zone 160 k (zone 3) is computedas a percentage of the pressure in seat zone 160 e (zone 2). Thepressures in seat zone 160 e and head zone 160 f are determined usingboth the transducers 328 and the pressure sensors 136. The pressures inone or more of the zones 160 may be adjusted in real time.

As shown in FIG. 5, fill valves 163 a-l and vent valves 165 a-l arecoupled to various portions of patient support 10 through third airlines 150 a, b, d-f, and g-l. Fill valve 163 a and vent valve 165 a arecoupled to upper foot bolsters 140 c, fill valve 163 b and vent valve165 b are coupled to lower side bolsters 142 a, b, fill valve 163 c iscoupled to atmosphere and vent valve 165 c is reserved for futuretherapies. Also, fill valve 163 d and vent valve 165 d are coupled tofirst turn assist 74 a, fill valve 163 e and vent valve 165 e arecoupled to seat bladders 62, fill valve 163 f and vent valve 165 f arecoupled to head bladder assembly 60, fill valve 163 g and vent valve 165g are coupled to foot filler 80, fill valve 163 h and vent valve 165 hare coupled to upper side bolsters 140 a, b, fill valve 163 i and ventvalve 165 i are coupled to deck filler 90, fill valve 163 j and ventvalve 165 j are coupled to first turn assist 74 b, fill valve 163 k andvent valve 165 k are coupled to foot bladders 164, fill valve 163 l andvent valve 165 l are coupled to lower foot bolsters 142 c. Vent valves165 d, j are biased in the open position to vent air from first andsecond turn assist 74 a, 74 b when first and second turn assist 74 a, 74b are not in use. Vent valves 165 d, j return to their open position ifthe mattress loses power or pressure venting air from the first andsecond turn assist 74 a, 74 b. When air is vented from a zone 160, thepressure in the zone 160 after deflation is determined by the controlsystem 42, 58 in real time rather than being predetermined.

In one embodiment, a user enters an input command to control unit 42.Control unit 42 processes the input command and transmits a controlsignal based on the input command through communication line 258 tocontrol board 250. Additionally or alternatively, control signals couldbe based on operational information from control unit 42 to increase ordecrease pressure within one or more of the zones 160 based oninformation obtained from transducers 328 and/or sensors 136.

It should be noted that in the illustrated embodiment, the mattresscontrols 42, 58 are independent from operation of the bed frame 4. Inother embodiments, however, bed frame 4 and mattress 10 may beconfigured to exchange or share data through communication lines. Forinstance, data may be communicated from bed frame 4 to mattress system42, 58 and used to adjust support parameters of mattress 10. Forinstance, in one embodiment, a signal is transmitted from frame 4 whenfoot section 34 is retracting, so that mattress systems 42, 58 respondsby decreasing internal pressure of vertical bladders 50 in foot assembly64.

As described above, air supply 152 is capable of supplying air or actingas a vacuum to remove air from zones 160. While in supply mode, amicroprocessor on control board 250 actuates corresponding fill valve163 a-l or vent valve 165 a-l based on the control signal from controlunit 42. For example, if the control signal indicates the pressure inhead bladder assembly 160 is to be increased fill valve 163 f isactuated. However, if the control signal indicates the pressure in headbladder assembly 160 is to be decreased vent valve 165 f is actuated.While in vacuum mode one or more fill valves 163 a-l may be actuated toallow for rapid removal of air within the corresponding zones.

FIG. 10 illustrates an overall system architecture 570 of a mattress inaccordance with the present invention. As previously described, themultiplexer board 508, also known as a sensor communication hub, iscoupled to the head zone sensor 68 and the seat zone sensor 70. Themultiplexer 508 as well as the optical system devices includes a numberof sensory algorithms to be described later herein. Also included in thesystem architecture 570 is the algorithm control unit 526 which includesa second set of sensory algorithms 574 and control algorithms 576. Theoutput of the multiplexer 508 and the algorithm control unit 526 arecoupled to a network 578 which is also coupled to the air control unit512 and the LCD display unit 44. The network 578 includes interfacehardware, also known as a communication hub. The network 578 acts as thecommunication bus for the various hardware, software, and firmwarecontrol devices.

As previously described, the multiplexer 508 includes the sensoryalgorithms 572. The algorithm control unit 526 also includes sensoryalgorithms which may include algorithms for providing pressure relief,for providing a motion metric, for providing weight estimation, and forproviding information to a LCD module which includes a calculation ofstatistics model.

FIG. 11 illustrates a block diagram of a control system 580incorporating the LCD display unit 44, the air control board 512, thecommunication hub or network 508, and the algorithm control unit 526.The communication hub 508 which receives sensor data from the head zonesensor 68 and the seat zone sensor 70 is coupled to both the LCD displayunit 44 and the algorithm control unit 526 through a first sensor dataline 582 and a second sensor data line 584 respectively. As describedwith respect to FIG. 10, the algorithm control unit 526 includes sensoryalgorithms 574 and control algorithms 576. The algorithm control unit526 includes a first output line 586 coupled to the LCD display unit 44for transmitting patient position monitor status, a second control line588 for communicating movement status, and a third control line 590 forcommunicating the status of the algorithm control unit. In addition, thealgorithm control unit 526 includes a fourth output line 592 whichtransmits the zone pressure boundary values for each of the head, seatand foot zones to the air control board 512 to which the line 592 iscoupled. The air control board 512, which includes the pressure sensorspreviously described, sends control pressure zone feedback signalsthrough a line 594 back to the algorithm control unit 526. The displayunit 44 through the user input interface device 524 also sends controlsignals to the algorithm control unit 526 through a control line 596which includes signals such as various mode command signals as well asbed type command signals for adjusting the frame or deck of the bed.

As previously described with reference to FIG. 10, the present inventionincludes sensory algorithms as well as control algorithms. The sensoryalgorithms are provided in firmware located within the multiplexer 508and the algorithm control unit 526. Sensory algorithms include thefollowing: bottom out detection, where a portion of the subject issupported by the bed frame as opposed to the surface, bed exitdetection, sitting on the side of a bed detection, detection of apatient lying on the edge of the surface, detecting a lack of patientmovement on the surface over a period of time, providing patientposition monitoring by distinguishing between the following sixpositions left lying, left sitting, center lying, center sitting, rightlying, right sitting, and measuring patient weight within plus or minus20% within the bed and the flat position. The control system algorithmswhich are located in the control system algorithm firmware 576 optimizepressure reduction by dynamic load distribution adjustment of thesurface air bladders of the mattress 10 located above the head sensorpad 68 and the seats sensor pad 70.

Referring now to FIG. 12, the illustrated embodiment of the control unit42 includes a housing 22. The exterior housing 22 includes a top end 26,a bottom end 28, a first side 92, and a second side 94. The exteriorhousing 22 defines an interior region containing control unit componentsto be described later herein.

A display portion 24 is pivotably coupled to the housing 22. Also showncoupled to the exterior housing 22 are a rotatable handle 98, a couplingassembly including first and second hangers 100, 102, an air filter 110,an electrical power input port 112, a power on/off switch 114, first andsecond feet 104, 106, and a cable 108. A visual indicator or light bar96 is also provided.

In FIG. 13, the display portion 24 is shown rotated upwardly into a useposition. Once placed in a use position, the display panel 116 may beeasily viewed by a caregiver. The display panel 116 is, in theillustrated embodiment, a liquid crystal display including a touchscreencontrol panel such that the user may simply touch the screen with afingertip in designated areas to give instructions for controlling thepatient support. As will be described later herein, the video displaypanel 116 is configured to be capable of displaying video clips and helpscreens, including videos that demonstrate operation, installation,and/or maintenance procedures for the patient support 10. All aspects ofthe user interface of display panel 116 are capable of being displayedin multiple languages, including, for example, English and Spanish. Thedisplay panel 116 is, in the illustrated embodiment an 8.4 inch highcontrast mode flip up LCD display screen.

Also provided on display portion 24 is an infrared (IRDA) port 118,which enables data collection and/or communication over a network usingwireless technology. For example, usage data regarding usage of themattress 10, and/or service information (i.e. how often the mattress hasbeen serviced) may be communicated to a remote computing device over awireless network through the use of the infrared port 118.

A memory port 120 is also provided in the display portion 24. Memoryport 120 is configured to removably receive memory cards such as compactflash memory, for example. SD memory cards, for example, may also beused, for example, in order to configure the control unit 42 withfirmware upgrades, changes to the software, or updates or additionaltraining or service videos. This eliminates the need to take the controlunit 42 out of service in order to accomplish these and other types ofupgrades and adjustments.

Also provided on display portion 24 are cover panels 122, 124, which areremovably coupled to exterior housing 128 of the display portion 24.Cover panels 122, 124 are generally made of the same material as therest of the exterior housing of display portion 24 (i.e.,polycarbonate). Cover panels 122, 124 are provided primarily to protectthe communication and data ports 118, 120 when those ports are not inuse. Cover panels 122, 124 may be coupled to exterior housing 128 by oneor more fasteners 126 (i.e., screws). Exterior housing 128 may alsoinclude a bracket configured to mate with a mating portion of afootboard, headboard, siderail or other similar port of a bed.

The usage data or service data that may be collected and transmittedthrough the infrared port 118 may include error logs or logs of themattress usage.

FIG. 14 shows a simplified exploded view of internal components of thedisplay portion 24. The front or top portion 128 of the exterior housingof display portion 24 is coupled to a back or bottom portion 130 by aseries of fasteners 132 through a series of apertures 134. A pivotcoupling assembly 194 includes a friction hinge 142 and a circularmember 138 which includes a plurality of spaced apart apertures 140. Ahollowed out semi-circular region of the display portion 24 includes afemale end 180 and a male end 178. The pivotable coupling assembly 194is position within the semi-circular region of the display portion 24 asshown by dashed lines 186, 188, and 190.

Corresponding female 184 and male 182 portions are provided in the upperend 26 of the exterior housing of the control unit 42. The pivotcoupling assembly 194 thereby mates with the coupling portions 182, 184as shown by dashed lines 186, 192. A suitable hinge 142 is the modelMH40 manufactured by Reell Precision Manufacturing Corporation of St.Paul, Minn. (www.reell.com). The hinge 142 allows the display portion 24to rotate between an upward or raised use position and a lowered orclosed storage position as described above. However, the display maybestopped at any position in between the two extreme positions. The rangeof motion of the pivotable display portion is greater than 180 degrees.

The video display 24 includes a front or top housing 128, and a back orbottom housing 130. Within the two housing portions, which define aninterior region, are provided a touchscreen 119 positioned above or ontop of a liquid crystal display assembly 115. An insulator (not shown)is provided between the LCD assembly 115 and the printed circuit boardor LCD board 121. An LCD cable 117 couples the display portion 24 to thealgorithm control board 196 through an opening in the male portion 178.

FIG. 15 shows the control unit 42 with the rear housing 234 removed toshow certain interior components of the control unit 42. The interiorcomponents of the control unit 42 include an algorithm control board526, a blower 198, a hose connector 200, a hose tubing 202 coupling thehose connector 200 to the blower 198, a pump or compressor 204, a valveassembly 206, and a power input assembly 208. These components aredescribed in greater detail below.

FIG. 16 illustrates a plurality of protective inserts 210, 212, 214which are provided within the interior region of control unit 42. Theinserts are aligned within the interior region of the control unit 42 asshown by dashed lines 216 and 218. Each of the inserts 210, 212, 214 ismade of an insulating material such as EPAC (Electronic PackagingAssembly Concept) foam. The EPAC foam provides an internal chassis forthe control unit 42. Each of the foam members 210, 212, 214 has withinit one or more cooling channels which allow air to circulate. Such airchannels (not shown) may also provide a channel for any leaking blowerair to escape. The inserts 210, 212, 214 also function to dampenstructural noise. In addition to the foam inserts 210, 212, 214,additional rubber mounting may also be provided, for example, on thecompressor 204, in order to improve noise and/or vibration performance.

FIGS. 17 and 18 show exploded views of interior components of thecontrol unit 42. In FIG. 17, the components are viewed from theperspective of a person looking at the front housing 232. In FIG. 18,the components are viewed from the opposite perspective. Referringparticularly to FIG. 17, front housing 232 includes the display portion24, visual indicator or light bar 96, and CPR button 30. The handle 98is pivotably coupled to the upper end 26 of the front housing 232.

The visual indicator or light bar 96 includes an LED lens 236, alightpipe 238, and LED board 240. The LED lens 236 provides a clearsurface for the LED light to penetrate. The lens may be textured orfrosted to adjust the dispersion of light. The LED lightpipe 238provides a path for the LED light to go through. The lightpipe 238 ismade of a molded plastic. In the illustrated embodiment, the lightpipe238 is divided into two parts for ease of moldability. The lightpipe 238may be textured or frosted to adjust the dispersion of the light. TheLED board 240 is coupled to the algorithm control board 196 to controlthe operation of the visual indicator or light bar 96.

The light bar 96 acts to visually alert a caregiver as to a situationinvolving the mattress 10, control unit 42, or patient, that may needattention. The light bar 96 may be illuminated in green, flashing green,or not illuminated at all, when the control unit and/or mattress isoperating normally. The light bar may be illuminated intermittently toindicate different modes of normal operation. For example, steady greenmay indicate pressure relief mode while flashing green may indicateanother mode (such as maxinflate, turn assist, etc.) A different mode(such as steady on flashing yellow or amber) may be used to indicatewhen either the control unit or the mattress is in need of service orwhen an alarm (such as a bed exit alarm, described elsewhere herein) isactivated. Yet another mode (such as steady or flashing red) may be usedto indicate that the CPR function of the mattress is turned on, that thepatient appears to be showing signs of inactivity or distress, or forother purposes. For example, the light bar 96 may be coupled to themotion monitor feature discussed elsewhere herein so that another visualalert is generated (an orange light, for example) if the patient'smotion is above or below an acceptable range. Also, the light bar 96 maybe coupled to one or more of the bed alarm settings discussed elsewhereherein so that a visual alert is generated if the patient is attemptingto exit the bed, or lying near the edge of the bed, for example.

The front housing 232 supports the foam insert 214, into which most ofthe interior components are loaded. The front housing 232 outlines andsupports the LED lens 236, light type 238, and holds the speaker 242 onits flange. The front housing 232 is made from Noryl structural foamsufficient to withstand applicable drop test requirements.

The handle 98 is attached to the front housing 232 by a pair of shoulderscrews. The handle is blow molded in polycarbonate. The algorithmcontrol board 526 is described elsewhere herein, for example withreference to FIGS. 7 and 19.

The air line 108 is coupled to the switching valve 206 by the inlet andoutlet tubing 244. Separate tubing 244 a, 244 b is provided for inletand outlet hoses.

The blower 198 is a commercially available blower such as Ametek modelno. 150166-00. The compressor 204 is a commercially available compressorsuch as Thomas model no. 6025SE-XP, part no. 950115. The switching valve206 is a pressure/vacuum valve such as is commercially available fromNumatics model no. 92114-2. The various pneumatic tubing used tointerconnect the pneumatic items in the control systems are generallyconventional pneumatic tubing. Also, various connectors and wiring areused to interconnect the electrical items in the control unit 42 and thepatient support 10. Rubber bumpers and screw caps are used to cover andhide screws and other fasteners on the control unit assembly. Aplurality of labels or label portions 332 (FIG. 12) are provided asneeded to meet marketing and regulatory requirements.

The power input 246 includes a power supply, for example XP model no.ECM130PS12, a power inlet, for example Corcom model no. PE0S0DBX0, and a120V power filter, such as Corcom model no. 3MZ1.

The foam inserts 210, 212 hold other components in place, for examplethe insert 212 keeps the blower, compressor, and power supply inposition, and the insert 210 keeps the power supply, speaker, and powerinlet in proper position. The insert 214 is also made of EPAC(Electronic Packaging Assembly Concept) foam and is used to hold thealgorithm control unit, compressor, blower, switching valve, and powersupply in place. The use of these foam inserts 210, 212, 214 eliminatesthe need for a metal chassis and fasteners.

The first and second end caps 248 conceal the screws and other moldingissues on the front and back housing 232, 234. The end caps are madefrom Santoprene Thermo Plastic Rubber (TPR). The end cap 248 alsoprovide cushioning for protection during impacts and drops. The firstend cap 248, positioned proximate to the friction hinge 142, alsoincludes a set of ribs to help keep the friction hinge in place. Itshould be noted that the housing portions 232, 234, 248 are interlockingwalls designed to prevent liquid ingress.

The filter holder 110 positions the foam air filter and maintains it infront of the air inlet ports on the front and back housing 232, 234. Thefilter 110 is molded in polycarbonate.

The hose receptacle 200 receives and holds the hose end. The receptacle200 also holds a gasket to prevent air leakage. Attached to thereceptacle are one or more air lines and electrical contacts (i.e.,three and eight, respectively, in the illustrated embodiment). Thereceptacle to 100 is made from Valox or another very strong material.The receptacle 200 is held in place by the front and back housings 232,234. The receptacle and corresponding hose are described in greaterdetail in U.S. Provisional Patent Application Ser. No. 60/636,252,assigned to the assignee of the present invention, and incorporatedherein by reference.

The hose itself includes the electrical contacts and air lines thatconnect directly to the patient support 10.

The rear housing portion 234 holds and compresses the back and side foaminsert 212, in order to hold all of the internal components in properposition. The rear housing 234 also provides mounting points for thehanger assembly 100, 102 and holds the speaker 242 in place. Rearhousing 234 is made from Noryl structural foam sufficient to withstandapplicable drop test requirements.

The control unit 42 may be attached to a footboard or other portion of abed frame, or may be positioned on the floor. Hook assemblies 100, 102are provided in order to attach the control unit 42 to a portion of abed, i.e., a footboard. The hooks are configured to support at leastfour times the weight of the control unit 42, without failing. Each ofthe hooks 100, 102 may be rotated or otherwise reconfigured in variouspositions in order to adapt to a variety of different footboards orother bed portions. A similar suitable hook assembly is described inU.S. Pat. No. 6,735,799 to Ellis, et al., assigned to the assignee ofthe present intervention and incorporated herein by this reference.

Feet 104, 106 are provided primarily to stabilize and protect thecontrol unit 42 when it is positioned on the floor. The feet 104, 106are made of rubber in the illustrated embodiment.

A pivot cover 222 is provided to hold the top pivots of the hookassemblies 100, 102 coupled to the rear housing 234. The cover 222 alsois adjustable to control the clearance between the cover 222 and thehooks 100, 102.

A rubber detent 330 is provided in order to hold the display portion 24in place, i.e., in the storage or downward position, for example duringtransport of the control unit 42. These detents 330 provide a resistanceto upward rotation of the display portion 24.

As noted above, the control unit 42 provides the user interface,mattress interface, mechanical system, and control for the mattress 10.FIG. 19 is a simplified system level block diagram for the control unit42. FIG. 19 shows the major components of the control unit 42, includingthe display board 528 and the algorithm board 526. In the illustratedembodiment, the display board 528 and algorithm board 526 provide thecontrol functions for the entire mattress system. The display board 528provides the primary interface between the end user, technician, orcaregiver and the mattress system. The display board 528 also containsthe mattress system's user interface.

In the illustrated embodiment, the user interface includes a touchscreenvideo display. The display board 528 is also capable of playing videofiles stored in a memory 550, using commercially available software suchas Windows Media Player. Such video files may be used, for exampleduring system installation and user training. The display board 528 isalso responsible for storing user data and providing access to that datavia its IRda infrared port 118. The display board interfaces to thealgorithm board 526 and to the rest of the mattress system via a CAN busconnection 552, 554.

The algorithm control board 526 controls the normal working of themattress system by executing algorithms that convert user requests intodesire actions. These algorithms may be executed, for example, to setproper mattress pressure distribution for a patient, detect patientposition, and/or provide patient turning assistance using the turnassist bladders 74.

As noted above the algorithm board 526 provides a CAN bus connection 552for other system components. The algorithm control board 526 alsoprovide speed control for the blower 198, which is used primarily formattress service cooling. The algorithm control board 526 also providespower for an ID tracking tag 544 and control of a pressure/vacuumswitching valve 540, which allows for inflation and quick deflation ofone or more portions of the mattress 10. The algorithm control board 526also provides switched AC power to the system's compressor 204 via anoptically isolated triac circuit. The CPR button 542 is also connectedto the algorithm board 526.

Electrically coupled to the display board 528 are the infrared port 118,the memory 550, the speaker 530, the touchscreen 524, the liquid crystaldisplay 546, and the backlight inverter 548.

The display board architecture is shown in more detail in FIG. 20. FIG.20 is a simplified block diagram for display board 528. The displayboard 528 includes a 32 bit microcontroller 556. In the illustratedembodiment an AMD Au1100 32 bit microcontroller is used. Other suitablemicroprocessors include the Intel Xscale and Freescale IDOTMX21. A CANmicrocontroller is coupled to the main microcontroller 556 in order toprovide the CAN function. In the illustrated embodiment the CANmicrocontroller 558 is an Atmel T89C51CC01. Coupled to the CANmicrocontroller 558 is a CAN transceiver 560. In the illustratedembodiment, the transceiver is a Philips TJA1054. The CAN controller 558communicates with the main microcontroller 556 through a UART. A levelshifting buffer function 562 is provided between these two devices.Optionally, the CAN controller 558 may also be used to vary the videodisplay's backlight brightness using one of its pulse width modulatedoutputs. The CAN controller 558 also provides a serial interface to thereal time clock of the display board 528.

As shown, a compact flash card or other suitable memory 550 may becoupled to the display board microcontroller 556. In this way, trainingvideos or other types of videos, for either or both a caregiver andtechnicians installing using or setting up a patient support 10 may bestored on removable flash memory cards which may be connected to themicrocontroller. The flash memory cards 550 may also provide a means forupdating software applications and the system operating system. Asuitable flash memory card is the Secure Digital (SD) card, however, theCompact Flash (CF) card also has the required capabilities and wouldwork equally as well. The display board 528 as shown will support eithera CF card or a SD card.

The primary function of the CAN microcontroller 558 of the display board528 is to translate CAN messages from the mattress system intoRS232-based messages for one of the display microcontroller 556, and toformat the display microcontroller's 556 serial messages into CANmessages and send them out on the CAN bus. The CAN microcontroller 558has a 80C51COR, 32 kilobytes of flash memory, 2 kilobytes of flashmemory for a bootloader, 2 kilobytes EEPROM storage for variables, and afull duplex UART. The real time clock is implemented by a Dallassemi-conductor DS 13O7Z, which is connected to the serial bus of the CANmicrocontroller 558. Power is provided to the real time clock by its ownindependent battery. The LCD backlight 548 is implemented using a PWMoutput of the CAN microcontroller 558. The reset of the displaymicrocontroller 556 is implemented by buffering an output of the CANmicrocontroller 558 to a reset pin of a supply voltage supervisor 564.

Development of a CAN microcontroller 558 may be accomplished usingstandard C programming and microcontroller emulation tools, as well asseveral commercially available CAN tools such as Micro Vision, Keil 8051software tools for C, and CANalyzer ProCAN. The CAN microcontroller 558acts as the protocol interface between the display board microcontroller556 and the rest of the mattress system. The CAN microcontroller 558provides firmware of great capabilities and also performs self test eachtime it is powered. The CAN microcontroller 558 is a pure-2-peer bus,therefore, all messages communicated are available to each component onthe bus. Each individual component, therefore, determines which CANmessages require its attention.

The touchscreen user interface 524 is a 5-wire overlay that iscontrolled by a peripheral controller. The peripheral controller 562controls the touchscreen and also provides a digital to analog converterfor the audio output to a power amplifier that drives the speaker 530.The peripheral controller is any controller that has both an audiodriver and a 5-wire touchscreen controller such as a Wolfson WM9712L.

A serial debug port 566 is provided for software debugging and also forpossible field upgrades, for example by a technician. A serial debugport 566 connects to a second UART port of the display microcontroller556.

An EJTAG port 568 is provided. The display microcontroller 556 utilizesthe EJTAG port 568 for program monitoring, debugging, and access to theMIPSCORE.

The IRda port 118 provides electrically isolated data transfer for thedisplay board 528. The infrared port 118 is built into the displaymicrocontroller 556 and supported in software.

The power of management circuitry 598 provides power-up and resetcircuitry for the display board 528. This circuitry is designed tocorrectly bring the display micro 556 out of a cold power up or out of awarm reset. The power of management circuitry 598 also regulates powerfor the peripheral devices CAN, memory, peripheral controller.

The display board 528 also include memory. The illustrated display board528 supports either or both 128 mega bits SDRAM and 64 mega bit flashmemory. The liquid crystal display 546 is, in the illustratedembodiment, a TFT VGA LCD (640.times.480) with a TTFL backlight.

A simplified block diagram for the algorithm board 526 is shown in FIG.21. The algorithm board 526 receives converted user directives receivedby the display board 528 and sent over to CAN bus 554. The algorithmboard 526 than takes the appropriate action by interacting with theremaining system components. In addition, the algorithm board 526directly controls the CPR button 542 and also a diagnostic LED light bar96, which may be used for trouble shooting on other purposes.

The microcontroller 604 for the algorithm board 526 is the Motorola FreeStyle MC9S12DJ128BCFU or other suitable 16-bit microcontroller with a128 killo bit flash EEPROM that can be upgraded to 256 killo bits ifnecessary. The algorithm control microcontroller 604 includes 8 killobits of RAM memory, 2 UART ports, and 7 eight-bit PWM channels also, thealgorithm control micro604 has a built in CAN controller, which supportsthe current versions of CAN.

The software for the algorithm board 526 was developed usingcommercially available development tools such as Code Warrier, MetroWerks Professional Edition C compiler. The algorithm control boardmicrocontroller 604 may also be a Renesas (Mitsubishi) M306N5FCTFP orRenesas, (Hitachi) HD64F2623. The algorithm control boardmicrocontroller 604 may be any other suitable microcontroller having therequired architecture, onchip in-application programming with flashmemory, ability to expand the memory without changing the host board,CAN channel, CAN drivers, and required drivers support.

The CAN bus connection 552 includes RJ-45 connectors for all systemresources that require access to the CAN bus. A Phillips TJA1054 CANtransceiver or other suitable CAN transceiver 606 is used to interfacethe microcontroller 604 to the CAN bus 552, 554.

Power is supplied by the mattress system to the algorithm board 526. Thealgorithm board linearly regulates the power supply for the board's ownlogic supply. The system's power supply is also linearly regulated forthe ID tracking tag 544. The algorithm 526 also distribute power to thedisplay board 526 sensor hub 508 and air control board 512.

As mentioned above, the blower 198 provides high volume low pressure aircirculating through a portion of the patient support 10. Themicrocontroller 604 controls the speed of the blower 198 through a PWMoutput 608. The algorithm control microcontroller 604 also providespower to the blower motor via a high current connection 610, which ismonitored by one of the microcontroller's A/D input. The microcontroller604 can disable the blower's power if an abnormal current is sensed.

The microcontroller 604 also controls and activates or deactivates thepressure/vacuum valve solenoid 206, which is located within the controlunit 42. The microcontroller output 612 are used to control a solenoiddriver which activates the switching valve 206. One GPIO pin is provideon the ground side of this solenoid and another GPIO pin is provided onthe high side of this solenoid. This high and low side control providesthe ability to turn off the solenoid, even if a single component failureoccurs in the driver circuit. PWM control of the high side switch alsoprovides the ability to duty-cycle and reduce the average solenoidcurrent, ‘once the solenoid has pulled in’.

Another output of the microcontroller 604 is used to control anoptically isolated triac switch 614 for the application of switched ACpower to the compressor 204. The triac circuit 614 also detects whenswitched AC is present and optically couples this information back to amicrocontroller input for monitoring purposes. A pressure sensor input616 is also connected to the microcontroller 604 as described above.

Referring back to FIG. 19, the touch screen 524 includes a resistive5-wire touchscreen which is used in connection with a liquid crystaldisplay 546. While less expensive 4-wire touchscreens may also be used,the 5-wire touchscreen is presently preferred. A suitable touchscreen isthe Elo Accutouch™ 8.4 inch touch screen part no. E24724-000. An Elo andIntellitouch surface way touchscreen may also be used.

As described above, the touchscreen 524 is used to display mattresscontrol information and options to a caregiver, technician, or other enduser, and receive as input directives from the end user. The remainingfigures show examples of user interface screens implemented usingtouchscreen 524.

FIGS. 22A and 22B illustrate user interface screens for a patientsupport that does not have a patient positioned upon it. In FIGS. 22Aand 22B, a graphical depiction of the patient support 622 indicates thatat the present moment, the head section of the patient support 10 israised. The user interface includes a first display portion 618 and asecond display portion 620. The graphical depiction of the patientsupport 622 is provided within the second display portion 620. The firstdisplay portion 618 includes a plurality of buttons 624, 626, 628, 630,632. Each of these buttons, in the illustrated embodiment, isactivatable by human touch or contact with another object. When one ofthese buttons is activated, an aspect of the button's presentation ormolding changes. For example, in FIG. 22A, a keylock button 626 isdarkened to show that the keylock button 626 is activated. When thekeylock button 626 is activated none of the other buttons are available.The buttons are indicated as not being available by a change in anaspect of the button's presentation, such as by being grayed out asshown. If the keylock button 626 is activated, then contact with any ofthe other buttons 624, 628, 630, 632 will not result in the associatedfunction being performed. Contact with the keylock button 626 when it isin the activated mode operates to deactivate the keylock and unlock thetouchscreen. The touchscreen 524 will then remain unlocked for a periodof time, for example 2 minutes, or until the keylock button 626, oranother button, is activated. When the touchscreen 524 is unlocked, thekeylock button 626 appears grayed out and the other available functionbuttons appear darkened. FIG. 22B shows the touchscreen 524 with thekeylock 626 turned off.

The menu button 624, if activated, brings up a plurality of additionalmenu options for controlling different features of the patient support10. The left and right turn assist buttons 628, 630 control the turnassist bladders 74A and 74B. Activation of the left turn assist button628 results in the left turn assist bladder being inflated to assist thecaregiver in rotating a patient positioned on the mattress 10.Activation of the right turn assist button 630 similarly activates theright turn assist bladder to rotate the patient in that direction.Activation of the maxinflate button 632 results in the patient support10 being over inflated, for example, for CPR therapy.

FIGS. 22C and 22D show similar touchscreen displays with the graphicaldepiction 622 of the patient support 10 shown in the horizontalposition, indicating that the mattress 10 or any portion thereof, is notelevated.

FIG. 23 shows a pull down menu that becomes active when the menu button624 is depressed. The pull down menu includes a plurality of menuoptions including alarm settings 636, motion monitor 638, surface map640, firmness override or “comfort adjust” 642, language 644, and inservice 646. Each of these menu options will be described below.

When the alarm settings button 636 is activated, a screen such as isshown in FIG. 24 is then displayed. The alarm settings portion of theuser interface is used for a caregiver or other enduser to configurevarious available alarms, which would alert a caregiver when the patientmay be moving into a position of danger. For example, a bed exit alarm648 is provided whereby the caregiver may configure the control unit 42to alert the caregiver when the patient appears to be preparing to exitthe bed. As shown in FIG. 24, there are a number of possible types ofbed exit alarms, including sitting up, sitting on the edge, and out ofbed. Thus, the caregiver can elect to be notified when the patient issitting up, when the patient appears to be sitting on the edge of thebed, or when the patient is already out of the bed. The buttons areactivated by contact, and when a button is activated, its presentationis changed as shown.

Another available alarm option is the edge-lying alarm 650. If theedge-lying alarm 650 is active, a caregiver will be notified when thepatient is laying up against the edge of the bed.

Once the caregiver has elected the desired alarm type, the caregiver canthen alter the alarm volume by pressing the plus or minus button 652. Agraphical display of molded bars indicates the relative loudness of thealarm. As described herein, the alarm is an audible signal, however, itcould also be a visual or electronic signal or other appropriate type ofalert. A similar adjustment for display screen brightness control mayalso be included.

FIGS. 25A-D show examples of pop up user interface windows that may bepresented in response to selection of a corresponding bed exit alarm.These pop up windows correspond to the selected button 648 shown on FIG.24. For example, when the sitting up button 648 is activated, thesitting up window shown in FIGS. 25A and 25C is presented to the enduser. The pop up window includes a silence button 654 and a reset button656. The silence button 654 is used to deactivate the alarm. The resetbutton 656 is used to reconfigure the alarm, or reset the alarmparameters to its previous settings. The pop up window shown in FIG. 25Ais displayed with the button 654, 656 darkened in as activated for aperiod of time, for example fifteen minutes, unless one of the buttonsis activated. If no button is activated after the period of timeexpires, then the buttons are deactivated as shown in FIG. 25B. FIGS.25C and D illustrate similar pop up windows for other available bed exitalarm selections. FIG. 25C illustrates a pop up window for the patientsitting on the edge of the bed alarm, and FIG. 25D illustrates a pop upwindow for the patient out of bed alarm. Note that the graphicaldepiction of the patient shown in the left hand portion of the pop upwindow changes depending upon the alarm type selected. If the sitting upbed exit alarm is selected, an alarm will sound when the patient movesaway from the head section of the mattress. Thus, the sitting up alarmis a more sensitive alarm as it typically alerts a caregiver when thepatient first begins to move.

When the sitting on the edge of the bed alarm is selected, an alarm willsound when the patient moves away from the center of the mattress towardan egress point. This setting typically alerts a caregiver when thepatient is preparing to exit the bed. The out of bed alarm will soundwhen the patient's presence is no longer detected by the mattress 10. Ifthe out of bed alarm is selected, the patient is able to move freelywithin the bed without triggering an alarm, but the caregiver is alertedif the patient leaves the bed.

FIGS. 26A-26B show similar user interface pop up windows that aredisplayed if the edge-lying alarm 650 is activated. When the edge-lyingalarm is selected, an alarm will sound when the patient is lying offcenter, on either edge of the bed. When this setting is used, thecaregiver is alerted if the patient may be lying against the side railsor appears to be in danger of rolling out of the bed.

The pop up windows shown in FIGS. 25C-25D illustrate a portion of themotion monitoring feature 638. In general, the motion monitoring featureenables caregivers to monitor the level of activity of a patient on themattress 10 over a period of time. For example, in FIG. 26C, a pop upwindow indicates that the patient's level of activity has been below athreshold motion monitoring level for a period of ninety minutes. Asconfigured, the caregiver was not alerted as to a change in thepatient's level of activity. The time period for triggering an alert maybe customized. The motion monitoring features are described in greaterdetail in U.S. patent application Ser. No. 11/119,635, filed May 2,2005, assigned to the assignee of the present invention and incorporatedherein by reference.

In the illustrated embodiment, the alarm settings and motion monitorportions of the user interface include graphical depictions illustratingthe particular feature, i.e., a person lying next to the edge of the bedin the case of the edge lying alarm. The graphical depiction changesdepending on the particular alarm setting or motion monitor featureselected.

FIG. 27 shows a user interface display 640 for a surface map 658. Thesurface map 658 is a real-time or snapshot graphical depiction of thedistribution of pressure applied to the surface 10. The legend 660 showsthat darker colors are indicative of higher pressure while lowerpressures are indicated by lighter colors in the illustrated embodiment.The example surface map 658 shown in FIG. 27 shows that pressure appearsto be concentrated in the center of the mattress 10. The surface map 658is updated in real time. For example, if a patient moves from a lyingdown position to a sitting position, the surface map will change to showa greater distribution of pressure in the seat section of the mattress.The surface map 658 may be used for clinical purposes, such as to allowan enduser to quickly assess a patient's risk of developing pressureulcers, by showing graphically the areas of higher pressure. The surfacemap 658 may also be used by service technicians, for example, toconfigure or troubleshoot the mattress. Access to the surface map 658may be restricted, for example, by requirement of a password.

In the illustrated embodiment, a firmness override or comfort adjustfeature 642 is also provided. The firmness override feature allows acaregiver to adjust the internal bladder pressure of one or more airbladders in the mattress 10 for patient comfort. For example, if aparticular patient prefers a firmer mattress, the internal bladderpressure may be increased. In the illustrated embodiment, the firmnessoverride feature is provided in addition to the automatic pressurerelief feature, but this may not always be the case. The firmnessoverride feature is described in more detail in U.S. Provisional PatentApplication Ser. No. 60/697,748, filed Jul. 8, 2005, and correspondingPCT Patent Application US2006/026788 filed on the same date herewith,assigned to the assignee of the present invention, and incorporatedherein by reference.

The language menu item 644 enables the end user to configure the controlunit user interface for a particular language, such as English, Spanish,or French.

The in service menu item 646 allows the end user to obtain informationrelated to servicing of the mattress 10.

FIGS. 28A-D show example user interface display screens relating to thefirmness override or comfort adjust feature 642. A graphical depictionof the mattress is provided, wherein one or more bars 672 are displayedwithin each portion of the mattress. The number wherein one or more bars672 are displayed within each portion of the mattress. The number ofbars corresponds to the relative internal pressure of the bladders inthat particular section of the mattress. For example, in FIG. 28A, thebladder pressure is greater in the head section of the mattress and thefoot section of the mattress and the pressure is lower in the seatsection of the mattress. FIGS. 28B and 28D illustrate that if a patientis positioned on the mattress 10, the graphical depiction of the bedchanges to include a patient. Also, if the head section of the mattressis elevated to an angle greater than thirty degrees, and a patient ispresent on the mattress 10, the graphical depiction changes again toindicate a no turn assist icon 676 and an angle indicator 674. The noturn assist icon 676 graphically indicates that the turn assist bladdersmay not be inflated while the mattress head angle is greater than thirtydegrees. The angle indicator 674 graphically indicates whether the headangle is less than or greater than thirty degrees as shown in FIGS. 28Band 28D. These graphical depictions allow a caregiver or other end userto quickly assess the situation of a patient using the mattress 10.Also, these graphical indications provide a simplified way tocommunicate information to caregivers and end users who may speakdifferent languages.

The in service menu item 646 also provides an online tutorial featurefor caregivers, service technicians, and other end users. FIGS. 29A and29B show examples of the online tutorial feature. In FIG. 29A, stillgraphics are provided to illustrate the use of the turn assist feature,for example. The graphics 662 are supplemented with text which providesan additional explanation. The end user can activate the show me button664 to view an online video demonstration of a selected bed feature.When the show me button 664 is activated, a video 666 relating to theselected feature (i.e., turn assist), is played. A pause button 670 anda replay button 668 are provided to allow the end user to pause theplaying of the video at any point or to replay the video.

FIGS. 30A-30F illustrate a sequence of example user interface displaysthat may be provided to communicate the status of an automatic pressurerelief feature of the mattress 10 to an end user. An example automaticpressure relief feature is described in greater detail in U.S. patentapplication Ser. No. 11/119,991, filed May 2, 2004, assigned to theassignee of the present invention, and incorporated herein by reference.The graphical nature of the display shown in FIGS. 30A-30F enables thecaregiver or other end user to quickly assess the status of the mattress10 and the patient positioned thereon, as noted above. In theillustrated embodiment, when a new patient is first placed upon themattress 10, the automatic pressure relief feature begins optimizing thepressure relief of the mattress 10 automatically. In FIG. 30A, the bars680 indicate which section or sections of the mattress 10 are beingoptimized. FIGS. 30B and 30C show an example user interface display whenthe patient's head angle is greater than thirty degrees from horizontal.FIGS. 30D-30F are similar graphical displays for a patient on a mattressthat is in the horizontal (unarticulated) position.

FIGS. 31A-31D show example user interface displays relating to the turnassist feature of the mattress 10. If a caregiver elects to activate oneof the turn assist buttons 628, 630, but the bed has side rails and theside rails are in the down position, a warning window 682 will appearprompting the caregiver to raise the side rails to their full positionbefore the turn assist feature will begin operating. FIG. 31Dillustrates a user interface display that is shown if the caregiverselects the left turn assist button 628. This display graphicallydepicts a patient 684 being rotated to the left. A similar graphicaldepiction is provided in FIG. 31C for activation of the right turnassist feature 630. If the caregiver attempts to activate the turnassist feature 628, 630, but the head of the mattress 10 is elevatedabove an angle of thirty degrees from horizontal, then a pop up windowsuch as shown in FIG. 31D is displayed. This display 686 includes anindication that the head angle of the mattress must be lowered belowthirty degrees in order for the turn assist feature to be utilized. Ifthe turn assist feature is already running when the head angle increasesabove thirty degrees, then the turn assist feature stops running. If thehead section of the mattress is at an angle of less than thirty degreesfrom the horizontal position then no pop up window is displayed and theturn assist feature can continue.

FIGS. 32A and 32B illustrate example graphical displays that would bepresented to an end user on the display portion 24 if the CPR button 30is activated or the maxinflate button 632 is activated. A message 688 isprovided to indicate to the caregiver that the CPR or max inflatefeature is in progress as shown in FIG. 32A. Once the CPR feature iscompleted, or after a period of time of no interaction, a second message690 is displayed indicating that the mattress will now return to itsstandard pressure relief mode.

FIG. 33 is an example of a user interface for initially configuring themattress 10, i.e, during installation. Such configuration is typicallydone by an authorized service technician. This screen and others may bepassword-protected or have access thereto otherwise restricted toauthorized personnel.

General site-specific information is displayed in window 692, such asthe type of bed frame on which the mattress 10 is being used, theservice number to call for questions or problems, and the defaultoperating mode for the mattress. In the illustrated embodiment, thedefault operating mode is the automatic pressure relief mode describedabove and also in U.S. patent application Ser. No. 11/119,991incorporated herein by reference. The automatic pressure relief mode maybe disabled, so that the mattress always maintains a preset bladderpressure, based on the patient's weight, for example.

FIG. 34 is an example of a user interface screen that may be displayedby control unit 42 for inputting a patient's weight. This screen may bepassword-protected or access otherwise restricted so that onlyauthorized personnel can enter a patient weight. As shown, a numerickeypad 706 and digital display of the patient's weight 708 are provided.An “enter” key or similar mechanism 710 is provided such that activationthereof (i.e. by human touch) causes the entered weight value to besaved into the system. A “lb/kg” toggle button or similar mechanism 712may be provided to enable entry of patient weight in either pounds orkilograms, or other suitable unit of measurement. A “clear” button 714may be provided to enable the entered weight value to be modified oredited before it is finalized.

Menu 698 displays a list of bed frame choices from which to select theappropriate frame. Once the bed type is selected, the mattress may beinflated by activation of button 694, and one or more aspects of thepressure relief system (if applicable) may be calibrated by activationof button 696, in accordance with the selected bed type. Video displaywindow 704 may display a video of a live demonstration to assist the enduser in understanding how to perform mattress configuration, service, orother procedures. Play and stop buttons 700, 702 are provided to enablethe end user to play or stop the video.

The present invention has been described with reference to certainexemplary embodiments, variations, and applications. However, thepresent invention is defined by the appended claims and therefore shouldnot be limited by the described embodiments, variations, andapplications.

The invention claimed is:
 1. A patient support apparatus comprising abed frame, control circuitry carried by the bed frame, the controlcircuitry receiving information about a plurality of conditions of thepatient support apparatus from sensors of different types that measuredifferent characteristics of the patient support apparatus, and a lightcoupled to the bed frame and coupled to the control circuitry, the lightbeing illuminated a first color in response to each condition of theplurality of conditions indicating that the patient support apparatus isoperating properly and the light being illuminated a second color,different than the first color, in response to the control circuitrydetecting an alert condition in any of the plurality of conditions, anda graphical display coupled to the bed frame and situated generallyvertically above the light.
 2. The patient support apparatus of claim 1,wherein the alert condition corresponds to a patient's amount of motionexceeding a threshold.
 3. The patient support apparatus of claim 1,wherein the alert condition corresponds to a patient attempting to exitthe patient support apparatus.
 4. The patient support apparatus of claim1, wherein the alert condition corresponds to a patient lying near anedge of the patient support apparatus.
 5. The patient support apparatusof claim 1, further comprising a foot board coupled to the bed frame andthe light is carried by the foot board.
 6. The patient support apparatusof claim 5, wherein the graphical display is carried by the foot boardabove the light.
 7. The patient support apparatus of claim 6, whereinthe graphical display comprises a touch screen.
 8. The patient supportapparatus of claim 7, further comprising a mattress supported on the bedframe and the touch screen displays icons that are used to controlfeatures of the mattress.
 9. The patient support apparatus of claim 1,wherein the first color is green.
 10. The patient support apparatus ofclaim 9, wherein the second color is amber or red.
 11. The patientsupport apparatus of claim 1, wherein the light flashes when beingilluminated the first color or the second color.
 12. The patient supportapparatus of claim 1, wherein the light comprises a lens and at leastone light producing element.
 13. The patient support apparatus of claim12, wherein the at least one light producing element includes aplurality of light producing elements.
 14. The patient support apparatusof claim 13, wherein the plurality of light producing elements includesa first light emitting diode (LED) that is operable to emit green lightand a second LED that is operable to emit red light.
 15. The patientsupport apparatus of claim 12, wherein the lens is frosted.
 16. Thepatient support apparatus of claim 12, wherein the lens is textured. 17.The patient support apparatus of claim 12, wherein the light furthercomprises a lightpipe through which light from the light producingelement passes before reaching the lens.
 18. The patient supportapparatus of claim 17, wherein the lightpipe is frosted.
 19. The patientsupport apparatus of claim 17, wherein the lightpipe is textured. 20.The patient support apparatus of claim 1, wherein the light isilluminated a third color when the patient support apparatus is in needof service.